meddevicedb.com FDA Device Reference

CONVALESCENT RECLINER

K802803 Class II Traditional
Decision Date
1980-11-19
Sponsor / Applicant
Winfield Co., Inc.

Technical Specification

510(k) Submission ID K802803
Product Code INO
Medical Specialty / Panel Physical Medicine
Regulation Citation 21 CFR 890.3110
Decision Date 1980-11-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CONVALESCENT RECLINER received FDA 510(k) clearance under submission number K802803, sponsored by Winfield Co., Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Physical Medicine review panel. The statutory decision date of record is 1980-11-19.

Classification & Regulation

This clearance is catalogued under FDA product code INO and 21 CFR 890.3110, within the Physical Medicine review panel as a Class II device.